23 results
·
22ms
·
Sources: EU EUDAMED, US FDA
ASAHI REXEED-SX/LX SERIES DIALYZER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Stansion Matrix®
FDA UDI
INNO Holdings, Inc.·M711B1214090·
Stansion Matrix®
FDA UDI
INNO Holdings, Inc.·M711C1214090·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973837·
BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code QJR·August 5, 2020
AT HOME OVULATION TEST, MODEL 9032
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SYSTEM IE LIQUID CHEMICAL CTERILANT PROCESSING SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1121409000·
Anterior Cervical IBFD EX
FDA UDI
KEOS·B084AC4121409070·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1121409040·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1121409070·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC2121409070·
Ascendant
FDA UDI
Choice Spine, LP·10885862260994·
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
UNKNOWN SECURE FIT MAX PLUS 7 X 11
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·June 7, 2011
ADVIA CENTAUR HIV 1/O/2 ENHANCED ASSAY
FDA Adverse Event
Other
·SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS INC.·Product code MZF·August 12, 2008
INCLUSIVE TAPERED IMPLANT
FDA Adverse Event
Malfunction
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 17, 2018
BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code QJR·July 14, 2020
PANTHER FUSION ADV/HMPV/RV ASSAY
FDA Adverse Event
Injury
·HOLOGIC INCORPORATED·Product code OCC·October 12, 2021
PANTHER FUSION SARS-COV-2 ASSAY PPR SOLUTION
FDA Adverse Event
Malfunction
·HOLOGIC INCORPORATED·Product code QJR·October 11, 2021